Synchronous medullary carcinoma and primary follicular lymphoma in the same thyroid lobe: a case report and literature review

Abstract Primary thyroid lymphoma (PTL) and medullary thyroid carcinoma (MTC) are rare malignancies. Their synchronous development as a collision tumor within a single thyroid lobe is exceptionally uncommon. We present a unique case of a 53-year-old female with a long-standing history of autoimmune thyroiditis who was simultaneously diagnosed with MTC and primary follicular lymphoma (FL, grade 3b) following histological examination of a surgical specimen. The diagnosis was confirmed using immunohistochemistry. Notably, the lymphoma cells lacked BCL2 expression despite a high histological grade, characteristic of a specific localized subgroup of extranodal FLs. This case highlights the critical importance of comprehensive histological and immunohistochemical evaluation of thyroid nodules, particularly in patients with chronic lymphocytic thyroiditis, to guide optimal therapeutic management.

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Publication Details

Journal
Journal of Rare Diseases
Published
2026-11-11
DOI
https://doi.org/10.1007/s44162-026-00257-4
Primary Topic
Thyroid Cancer Diagnosis and Treatment
Type
article
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article

Synchronous medullary carcinoma and primary follicular lymphoma in the same thyroid lobe: a case report and literature review

Liliya S. Urusova, Konovalov Dmitry, Пачуашвили Нано Владимеровна, A. V. Varlamov et al.
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Journal of Rare Diseases
Thyroid Cancer Diagnosis and Treatment
article

Synchronous medullary carcinoma and primary follicular lymphoma in the same thyroid lobe: a case report and literature review

Liliya S. Urusova, Konovalov Dmitry, Пачуашвили Нано Владимеровна, A. V. Varlamov, Dmitry Abramov, Elizaveta Churilova
article en

Abstract

Abstract Primary thyroid lymphoma (PTL) and medullary thyroid carcinoma (MTC) are rare malignancies. Their synchronous development as a collision tumor within a single thyroid lobe is exceptionally uncommon. We present a unique case of a 53-year-old female with a long-standing history of autoimmune thyroiditis who was simultaneously diagnosed with MTC and primary follicular lymphoma (FL, grade 3b) following histological examination of a surgical specimen. The diagnosis was confirmed using immunohistochemistry. Notably, the lymphoma cells lacked BCL2 expression despite a high histological grade, characteristic of a specific localized subgroup of extranodal FLs. This case highlights the critical importance of comprehensive histological and immunohistochemical evaluation of thyroid nodules, particularly in patients with chronic lymphocytic thyroiditis, to guide optimal therapeutic management.

Journal of Rare DiseasesVol. 5(1)
Sechenov University (RU), Endocrinology Research Center (RU), Russian Cancer Research Center NN Blokhin (RU), Ministry of Health of the Russian Federation (RU), Dmitry Rogachev National Research Center of Pediatric Hematology, Oncology and Immunology (RU)
Good health and well-being
Thyroid Cancer Diagnosis and Treatment
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